Copper complexes for optoelectronic applications

ABSTRACT

The invention relates to an optoelectronic component having a copper(I) complex of the formula: 
                         
wherein X is independently selected from Cl, Br and I; N*∩E or E∩N* is a bidentate ligand connected to a first Cu atom via an N atom and connected to a second Cu atom via an E group, or a monodentate ligand connected to a Cu atom via an E group, wherein E is R 2 As or R 2 P, wherein R is selected from alkyl, aryl, alkoxy, and phenoxy; N* is a part of an aromatic group comprising an imine functional group, wherein the aromatic group is selected from pyridyl, pyrimidyl, pyridazinyl, triazinyl, oxazolyl, thiazolyl, imidazolyl, and fused N-heteroaromatics, and wherein the imine functional group comprises the N atom double bonded to a carbon atom of the aromatic group; and ∩ is a carbon atom, which is likewise part of the aromatic group, connected to the N atom of said aromatic group and also connected to the E group via the As or P atom of the E group.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a Divisional of U.S. patent application Ser. No.13/380,361, filed on Apr. 5, 2012, which claims the benefit ofInternational Patent Application No. PCT/EP2010/059012 filed on Jun. 24,2010 and German Patent Application No. 102009030475.4 filed on Jun. 24,2009, the disclosures of which are incorporated herein by reference intheir entireties.

TECHNICAL FIELD

The invention relates to copper(I) complexes of the general formula A,especially for use in optoelectronic components.

BACKGROUND OF THE INVENTION

A dramatic change is currently on the horizon in the sector of visualdisplay unit and illumination technology. It will become possible tomanufacture flat displays or illuminated surfaces with a thickness ofless than 0.5 mm. These are notable for many fascinating properties. Forexample, it will be possible to achieve illuminated surfaces in the formof wallpaper with very low energy consumption. In addition, color visualdisplay units with hitherto unachievable trueness of color, brightnessand viewing angle independence will be producible with low weight andvery low power consumption. The visual display units will beconfigurable as microdisplays or large visual display units of severalm² in area, in rigid or flexible form, or else as transmission orreflection displays. In addition, it will be possible to use simple andinexpensive production processes such as screenprinting or inkjetprinting or vacuum sublimation. This will enable very inexpensivemanufacture compared to conventional flat visual display units. This newtechnology is based on the principle of OLEDs, Organic Light EmittingDiodes, which is shown schematically and in simplified form in FIG. 1.

Such components consist predominantly of organic layers, as shownschematically and in simplified form in FIG. 1. At a voltage of, forexample, 5 V to 10 V, negative electrons pass from a conductive metallayer, for example from an aluminum cathode, into a thin electronconduction layer and migrate in the direction of the positive anode.This consists, for example, of a transparent but electrically conductivethin indium tin oxide layer, from which positive charge carriers, calledholes, migrate into an organic hole conduction layer. These holes movein the opposite direction compared to the electrons, specifically towardthe negative cathode. In a middle layer, the emitter layer, whichlikewise consists of an organic material, there are additionally specialemitter molecules at which, or close to which, the two charge carriersrecombine and lead to uncharged but energetically excited states of theemitter molecules. The excited states then release their energy asbright emission of light, for example in a blue, green or red color.White light emission is also achievable. In some cases, it is alsopossible to dispense with the emitter layer when the emitter moleculesare present in the hole or electron conduction layer.

The novel OLED components can be configured with a large area asillumination bodies, or else in exceptionally small form as pixels fordisplays. A crucial factor for the construction of highly effectiveOLEDs is the luminous materials used (emitter molecules). These can beimplemented in various ways, using purely organic or organometallicmolecules, and complexes. It can be shown that the light yield of theOLEDs can be much greater with organometallic substances, called tripletemitters, than for purely organic materials. Due to this property, thefurther development of the organometallic materials is of highsignificance. The function of OLEDs has been described veryfrequently.^([i-vi]) Using organometallic complexes with high emissionquantum yield (transitions including the lowermost triplet states to thesinglet ground states), it is possible to achieve a particularly highefficiency of the device. These materials are frequently referred to astriplet emitters or phosphorescent emitters. This has been known forsome time)^([i-v])For triplet emitters, many property rights havealready been applied for and granted.^([vii-xix])

Copper complexes of the Cu₂X₂L₄, Cu₂X₂L′₂ and Cu₂X₂L₂L′ form(L=phosphine, amine, imine ligand; L′=bidentate phosphine, imine, amineligand, see below) are already known from the prior art. They exhibitintense luminescence on excitation with UV light. The luminescence canoriginate from an MLCT, CC (cluster centered) or XLCT (halogen-to-ligandcharge transfer) state, or a combination thereof. Further details ofsimilar Cu(I) systems can be found in the literature.^([xx]) In the caseof the related [Cu₂X₂(PPh₃)₂nap] complex (nap=1,8-naphthyridine, X=Br,I), a transition between the molecular orbital of the {Cu₂X₂} unit (Cu dand halogen p orbitals) and the π* orbitals of the nap group isdiscussed.^([xxi])

orbitals of the nap group is discussed.

Triplet emitters have great potential for generation of light indisplays (as pixels) and in illuminated surfaces (for example asluminous wallpaper). Very many triplet emitter materials have alreadybeen patented, and are now also being used technologically in firstdevices. The solutions to date have disadvantages and problems,specifically in the following areas:

-   -   long-term stability of the emitters in the OLED devices,    -   thermal stability,    -   chemical stability to water and oxygen,    -   availability of important emission colors,    -   manufacturing reproducibility,    -   achievability of high efficiency at high current densities,    -   achievability of very high luminances,    -   high cost of the emitter materials,    -   emitter materials are toxic and    -   syntheses are complex.

Against this background, it was an object of the present invention toovercome at least some of the abovementioned disadvantages.

SUMMARY OF THE INVENTION

The invention provides an optoelectronic component comprising acopper(I) complex of the formula A

X=independently selected from Cl, Br and I; N*∩E or E∩N*=a bidentateligand connected to a first Cu atom via an N atom and connected to asecond Cu atom via an E group, or a monodentate ligand connected to a Cuatom via an E group wherein: E=R2As or R2P, wherein R is selected fromthe group consisting of alkyl, aryl, alkoxy, and phenoxy; N*=part of anaromatic group comprising an imine functional group, wherein thearomatic group is selected from pyridyl, pyrimidyl, pyridazinyl,triazinyl, oxazolyl, thiazolyl, imidazolyl, and fused N-heteroaromatics,and wherein the imine functional group comprises the N atom doublebonded to a carbon atom of the aromatic group; and ∩=a carbon atom,which is likewise part of the aromatic group, connected to the N atom ofsaid aromatic group and also connected to the E group via the As or Patom of the E group, and wherein N*∩E or E∩N* optionally has at leastone substituent to increase the solubility of the copper(I) complex inan organic solvent.

BRIEF DESCRIPTION OF THE DRAWINGS

Exemplary embodiments of the present invention will be described belowin more detail, with reference to the accompanying drawings, of which:

FIG. 1 is a schematic and simplified diagram of the mode of function ofan Organic Light Emitting Diode (OLED) (the layers applied are, forexample, only approx. 300 nm thick);

FIG. 2 illustrates a solid-state structure of ligand 2;

FIG. 3 illustrates a solid-state structure of ligand 3;

FIG. 4 illustrates a solid-state structure of compound 4a;

FIG. 5 illustrates a solid-state structure of compound 4c;

FIG. 6 shows an emission spectra of solid crystalline samples ofcompounds 4a-4c (excitation at 380 nm);

FIG. 7 illustrates a component of the solid-state structure of compound5c;

FIG. 8 shows an emission spectra of solid crystalline samples ofcompounds 5a-5c (excitation at 380 nm);

FIG. 9 illustrates a component of the solid-state structure of compound6c;

FIG. 10 shows an emission spectrum of a solid crystalline sample ofcompound 6c (excitation at 420 nm);

FIG. 11 shows an emission decay curve of compound 6c at 300 K,excitation 420 nm;

FIG. 12 illustrates calculated frontier orbitals of the base state ofcompound 4c;

FIG. 13 is a simplified block diagram of an example of an Organic LightEmitting Diode (OLED) device with an inventive emitter layer, whichshould be applied by wet-chemical means. The layer thickness in thefigures should be regarded as exemplary values for purposes ofillustration, and is not necessarily to drawn to scale;

FIG. 14A illustrates the crystal structure of compound 8;

FIG. 14B shows the emission spectrum of compound 8, and morespecifically, an emission spectrum of a solid sample of compound 8(halogen=I) as a film on glass substrate at 300K, excitation at 355 nm,and emission maximum at 551 nm;

FIG. 15 shows an emission spectrum of a solid sample of compound 10(halogen=I) as a film on glass substrate at 300K, excitation at 355 nm,and emission maximum at 551 nm;

FIG. 16 shows an emission spectrum of a solid sample of compound 12(halogen=I) as a film on glass substrate at 300K, excitation at 355 nm,and emission maximum at 551 nm;

FIG. 17 shows an emission spectrum of a solid sample of compound 14(halogen=I) as a film on glass substrate at 300K, excitation at 355 nm,and emission maximum at 551 nm;

FIG. 18 shows an emission spectrum of a solid sample of compound 16(halogen=I) as a film on glass substrate at 300K, excitation at 355 nm,and emission maximum at 550 nm;

FIG. 19 shows an emission spectrum of a solid sample of compound 18(halogen=I) as a film on glass substrate at 300K, excitation at 355 nm,and emission maximum at 552 nm;

FIG. 20A illustrates a crystal structure of compound 20;

FIG. 20B shows an emission spectrum of a solid sample of compound 20(halogen=I) as a film on glass substrate at 300 K, excitation at 355 nm,and emission maximum at 521 nm;

FIG. 21A illustrates a crystal structure of compound 22;

FIG. 21B shows an emission spectrum of a solid sample of compound 22(halogen=I) as a film on glass substrate at 300 K, excitation at 355 nm,and emission maximum at 561 nm;

FIG. 22A illustrates a crystal structure of compound 28;

FIG. 22B shows an emission spectrum of a solid sample of compound 28(halogen=I) as a film on glass substrate at 300 K, excitation at 355 nm,and emission maximum at 574 nm;

FIG. 23 shows an emission spectrum of a solid sample of compound 30(halogen=I) as a film on glass substrate at 300K, excitation at 355 nm,and emission maximum at 572 nm;

FIG. 24 shows an emission spectrum of a solid sample of compound 32(halogen=I) as a film on glass substrate at 300K, excitation at 355 nm,emission maximum at 597 nm; and

FIG. 25 shows an emission spectrum of a solid sample of compound 34(halogen=I) as a film on glass substrate at 300K, excitation at 355 nm,and emission maximum at 679 nm.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS OF THE INVENTION

Exemplary embodiments of the invention will now be discussed in furtherdetail. This invention may, however, be embodied in many different formsand should not be construed as limited to the embodiments set forthherein.

The problem underlying the invention is solved by the provision ofcopper(I) complexes of the Cu₂X₂(E∩N*)₃ form, which have a structure ofthe formula A:

wherein:

X=Cl, Br and/or I (i.e. independently, such that the complex may havetwo identical or two different X atoms),

E=R₂As and/or R₂P,

N*∩E=bidentate ligands wherein E=phosphinyl/arsenyl radical of the R₂Eform (R=alkyl, aryl, alkoxy, phenoxy, amide); N*=imine function. “∩” isa carbon atom. More particularly, E is a Ph₂P group (Ph=phenyl); theimine function is part of an aromatic group (e.g. pyridyl, pyrimidyl,pyridazinyl, triazinyl, oxazolyl, thiazolyl, imidazolyl, etc.). “∩” islikewise part of this aromatic group. The carbon atom is directlyadjacent both to the imine nitrogen atom and to the E atom. N*∩E mayoptionally be substituted, especially by groups which increase thesolubility of the copper(I) complex in the standard organic solvents forOLED component production. Standard organic solvents include, as well asalcohols, ethers, alkanes and halogenated aliphatic and aromatichydrocarbons and alkylated aromatic hydrocarbons, especially toluene,chlorobenzene, dichlorobenzene, mesitylene, xylene, tetrahydrofuran.

An inventive copper(I) complex consists preferably of three identicalligands N*∩E, which reduces the synthesis complexity and hence the costsof preparation. The great advantage in the case of use of copper as thecentral metal is the low cost thereof, in particular compared to themetals such as Re, Os, Ir and Pt which are otherwise customary in OLEDemitters. In addition, the low toxicity of copper also supports usethereof.

With regard to use thereof in optoelectronic components, the inventivecopper(I) complexes are notable for a wide range of achievable emissioncolors. In addition, the emission quantum yield is high, especiallygreater than 50%. For emitter complexes with a Cu central ion, theemission decay times are astonishingly short.

In addition, the inventive copper(I) complexes are usable in relativelyhigh emitter concentrations without notable quenching effects. Thismeans that emitter concentrations of 5% to 100% can be used in theemitter layer.

Preferably, the ligand N*∩E comprises the following ligands:

wherein

Y=O, S or NR5

E*=As or P

R1-R5 may each independently be hydrogen, halogen or substituents bondedvia oxygen or nitrogen, or else alkyl, aryl, heteroaryl, alkenyl,alkynyl, trialkylsilyl and triarylsilyl groups, or substituted alkyl,aryl, heteroaryl and alkenyl groups with substituents such as halogens,lower alkyl groups. The R1-R5 groups may also lead to fused ring systems(for example ligand 3 shown below).

The invention also relates to a process for preparing an inventivecopper(I) complex. This process according to the invention has the stepof performance of a reaction of N*∩E with Cu(I)X, wherein

X=(independently) Cl, Br or I

N*∩E=a bidentate ligand where

-   -   E=phosphinyl/arsenyl radical of the form R₂E (where R=alkyl,        aryl, alkoxy, phenoxy or amide);    -   N*=imine function which is part of an aromatic group selected        from pyridyl, pyrimidyl, pyridazinyl, triazinyl, oxazolyl,        thiazolyl and imidazolyl,

“∩”=at least one carbon atom which is likewise part of the aromaticgroup, wherein the carbon atom is directly adjacent both to the iminenitrogen atom and to the phosphorus or arsenic atom. The at least onesubstituent optionally present on the ligand N*∩E to increase thesolubility of the complex in organic solvents is described below.

The reaction is preferably performed in dichloromethane (DCM). Theaddition of diethyl ether to the dissolved product allows a solid to beobtained. The latter can be conducted by precipitation or inwarddiffusion or in an ultrasound bath.

The reaction of bidentate P∩N* ligands (P∩N*=phosphine ligand, fordefinition see below) with Cu(I)X (X=Cl, Br, I), preferably indichloromethane (DCM), preferably at room temperature, surprisinglyforms—even in the case of a nonstoichiometric ratio—the biccylic 2:3complex Cu₂X₂(P∩N*)₃ in which the copper atoms are bridged by aphosphine ligand and the two halide anions (eq. 1).

The structure of the formula A is related to known complexes of theCu₂X₂L₂L′ or Cu₂X₂L₄ form. Unlike the case of Cu₂X₂L₂L′, the complex,however, is obtainable in only one step by reaction of Cu(I)X with thebidentate P∩N* ligand. The complex can be isolated by precipitation withEt₂O as a yellow or red microcrystalline powder. Single crystals can beobtained by slow diffusion of Et₂O into the reaction solution. As soonas the complexes are present as powders or crystals, they are sparinglysoluble to insoluble in common organic solvents. Especially at lowsolubilities, complexes were identified only by elemental and X-raystructural analyses.

This is the general formula A shown above. The bidentate E∩N* ligandsmay each independently include at least one substituent: thesubstituents may each independently be hydrogen, halogen or substituentsbonded via oxygen or nitrogen, or else alkyl, aryl, heteroaryl, alkenyl,alkynyl, trialkylsilyl and triarylsilyl groups, or substituted alkyl,aryl, heteroaryl and alkenyl groups with substituents such as halogens,lower alkyl groups. The substituents may also lead to fused ringsystems.

The preparation process may optionally include the step of substitutingat least one ligand N*∩E with at least one substituent to increase thesolubility in an organic solvent, wherein the substituent in oneembodiment of the invention may be selected from the group consistingof:

-   -   long-chain, branched or unbranched or cyclic alkyl chains of        length C1 to C30,    -   long-chain, branched or unbranched or cyclic alkoxy chains of        length C1 to C30,    -   branched or unbranched or cyclic perfluoroalkyl chains of length        C1 to C30, and    -   short-chain polyethers.

The invention also includes copper(I) complexes preparable by such asynthesis process.

According to the invention, the copper(I) complexes of the formula A canbe used as emitter materials involving the triplet state in an emitterlayer of a light-emitting optoelectronic component.

According to the invention, the copper(I) complexes of the formula A canalso be used as absorber materials in an absorber layer of anoptoelectronic component.

The expression “optoelectronic components” is understood to meanespecially:

-   -   organic light-emitting diodes (OLEDs),    -   light-emitting electrochemical cells (LECs, LEECs),    -   OLED sensors, especially in gas and vapor sensors without        hermetic shielding on the outside,    -   organic solar cells (OSCs, organic photovoltaics, OPVs),    -   organic field-effect transistors and    -   organic lasers.

The proportion of the copper(I) complex in the emitter or absorber layerin such an optoelectronic component is, in one embodiment of theinvention, 100%. In an alternative embodiment, the proportion of thecopper(I) complex in the emitter or absorber layer is 1% to 99%.

Advantageously, the concentration of the copper(I) complex as an emitterin optical light-emitting components, especially in OLEDs, is between 1%and 10%.

The present invention also provides optoelectronic components whichcomprise a copper(I) complex described here. The optoelectroniccomponent may be in the form of an organic light-emitting component, anorganic diode, an organic solar cell, an organic transistor, an organiclight-emitting diode, a light-emitting electrochemical cell, an organicfield-effect transistor and an organic laser.

The present invention further relates to a process for producing anoptoelectronic component, wherein an inventive copper(I) complex of thetype described here is used. In this process, more particularly, aninventive copper(I) complex is applied to a carrier. This applicationcan be effected by wet-chemical means, by means of colloidal suspensionor by means of sublimation.

The present invention also relates to a process for altering theemission and/or absorption properties of an electronic component. Thisinvolves introducing an inventive copper(I) complex into a matrixmaterial for conduction of electrons or holes into an optoelectroniccomponent.

The present invention also relates to the use of an inventive copper(I)complex, especially in an optoelectronic component, for conversion ofLTV radiation or of blue light to visible light, especially to green(490-575 nm), yellow (575-585 nm), orange (585-650 nm) or red light(650-750 nm) (down-conversion).

Since some of the inventive copper(I) complexes with unsubstituted N*∩Eligands are sparingly soluble in some organic solvents, they may not beprocessable directly from solution. In the case of solvents which arethemselves good ligands (acetonitrile, pyridine), a certain solubilityexists, but a change in the structure of the complexes or displacementof the phosphine or arsine ligands under these conditions cannot beruled out. It is therefore unclear whether the substances, in the eventof deposition on the substrate, will crystallize as Cu₂X₂(E∩N*)₃, orwill be present molecularly in this form in the matrix. For this reason,the substances should be produced in a size suitable for use inoptoelectronic components or be comminuted thereto (<20 nm to 30 nm,nanoparticles), or be rendered soluble by means of suitablesubstituents.

The inventive copper(I) complexes are preferably processed fromsolution, since the high molecular weight complicates deposition fromvacuum by sublimation. Thus, the photoactive layers are preferablyproduced from solution by spin-coating or slot-casting processes, or byany printing process such as screenprinting, flexographic printing,offset printing or inkjet printing.

The unsubstituted copper(I) complexes 4a, 4b, 4c, 5a, 5b, 5c, 6a, 6b,and 6c described here (defined below, see examples) are, however,sparingly soluble in the standard organic solvents, except indichloromethane, which should not be used for OLED component productionin a glovebox. Application as a colloidal suspension is viable in manycases (see below), but industrial processing of the emitter materials indissolved form is usually simpler in technical terms. It is therefore afurther aim of this invention to chemically alter the emitters such thatthey are soluble. Suitable solvents for the OLED component productionare, as well as alcohols, ethers, alkanes and halogenated aromatic andaliphatic hydrocarbons and alkylated aromatic hydrocarbons, especiallytoluene, chlorobenzene, dichlorobenzene, mesitylene, xylene,tetrahydrofuran.

In order to improve the solubility of the inventive copper(I) complexesin organic solvents, at least one of the N*∩E structures is preferablysubstituted by at least one substituent. The substituent may be selectedfrom the group consisting of:

-   -   long-chain, branched or unbranched or cyclic alkyl chains with a        length of C1 to C30, preferably with a length of C3 to C20, more        preferably with a length of C5 to C15,    -   long-chain, branched or unbranched or cyclic alkoxy chains with        a length of C1 to C30, preferably with a length of C3 to C20,        more preferably with a length of C5 to C15,    -   branched or unbranched or cyclic perfluoroalkyl chains with a        length of C1 to C30, preferably with a length of C3 to C20, more        preferably with a length of C5 to C15, and    -   short-chain polyethers, for example polymers of the        (—OCH₂CH₂O—)_(n) form wherein n<500. Examples thereof are        polyethylene glycols (PEGs), which can be used as chemically        inert, water-soluble and nontoxic polymers with a chain length        of 3-50 repeat units.

In a preferred embodiment of the invention, the alkyl chains or alkoxychains or perfluoroalkyl chains have been modified with polar groups,for example with alcohols, aldehydes, acetals, amines, amidines,carboxylic acids, carboxylic esters, carboxamides, imides, carbonylhalides, carboxylic anhydrides, ethers, halogens, hydroxamic acids,hydrazines, hydrazones, hydroxylamines, lactones, lactams, nitriles,isocyanides, isocyanates, isothiocyanates, oximes, nitrosoaryls,nitroalkyls, nitroaryls, phenols, phosphoric esters and/or phosphonicacids, thiols, thioethers, thioaldehydes, thioketones, thioacetals,thiocarboxylic acids, thioesters, dithio acids, dithio esters,sulfoxides, sulfones, sulfonic acids, sulfonic esters, sulfinic acids,sulfinic esters, sulfenic acids, sulfenic esters, thiosulfinic acids,thiosulfinic esters, thiosulfonic acids, thiosulfonic esters,sulfonamides, thiosulfonamides, sulfinamides, sulfenamides, sulfates,thiosulfates, sultones, sultams, trialkylsilyl and triarylsilyl groups,and also trialkoxysilyl groups which result in a further increase insolubility. The substituents of the N*∩E structures of the copper(I)complexes may be arranged anywhere in the structure. More particularly,a position of the substituent in the ortho, meta and/or para position tothe heteroatom which forms the coordination to the copper ion ispossible. Preference is given to substitution in the meta and/or paraposition.

A very marked increase in solubility is achieved from at least one C4unit, branched or unbranched or cyclic. Substitution, for example, witha linear C7 chain in 14 (see below) leads to a very good solubility in,for example, dichlorobenzene and to good solubility in chlorobenzene andtoluene.

A further aspect of the invention relates to the alteration of theemission colors of the copper(I) complexes by means of electron-donatingor -withdrawing substituents, or by means of fused N-heteroaromatics.The terms “electron-donating” and “electron-withdrawing” are known tothose skilled in the art.

Examples of electron-donating substituents are especially:

-alkyl, -phenyl, —CO₂(−), —O(−), —NH-alkyl group, —N-(alkyl group)₂,—NH₂, —OH, —O-alkyl group, —NH(CO)-alkyl group, —O(CO)-alkyl group,—O(CO)-aryl group, —O(CO)-phenyl group, —(CH)═C-(alkyl group)₂, —S-alkylgroup.

Examples of electron-withdrawing substituents are especially:

-halogen, —(CO)H, —(CO)-alkyl group, —(CO)O-alkyl group, —(CO)OH,—(CO)halide, —CF₃, —CN, —SO3H, —NH₃(+), —N(alkyl group)₃(+), —NO₂.

Advantageously, the electron-donating and -withdrawing substituents areas far as possible removed from the coordination site of the ligand, andare especially in the meta or para position.

Electron-donating substituents lead, by increasing the LUMO, to a changein the emission color of the copper(I) complexes in the direction of theblue spectral region (example: 20 (see below), substitution by means ofan NMe₂ unit).

Electron-withdrawing substituents lead, by lowering the LUMO, to achange in the emission color of the copper(I) complexes in the directionof the yellow-red spectral region (example: 30 (see below), theintroduction of a fluorine atom in the 5 position of the pyridine).

It is thus possible, through suitable selection of substitution withinthe base structure of a pyridine ligand, to establish a very broademission color range.

The change in the emission colors of the copper(I) complexes describedhere can also be effected by further heteroatoms such as N, O, S, and bymeans of fused N, O and S heteroaromatics.

The use of fused N-heteroaromatics (for example isoquinoline 6,benzothiazole 28, quinoxaline 34, see explanations further down) enablescolor shifts, for example into the yellow to deep-red spectral range.The solubility of copper(I) complexes with fused N-heteroaromatics canlikewise be increased by substitution(s) with the above-describedsubstituents, long (branched or unbranched or cyclic) alkyl chains oflength C1 to C30, preferably with a length of C3 to C20, more preferablywith a length of C5 to C15, long (branched or unbranched or cyclic)alkoxy chains of length C1 to C30, preferably with a length of C3 toC20, more preferably with a length of C5 to C15, long (branched orunbranched or cyclic) perfluoroalkyl chains of length C1 to C30,preferably with a length of C3 to C20, more preferably with a length ofC5 to C15, and short-chain polyethers (chain length: 3-50 repeat units).

In a preferred embodiment, the inventive copper(I) complex has at leastone substituent to increase solubility in an organic solvent and/or atleast one electron-donating and/or at least one electron-withdrawingsubstituent. It is also possible that a substituent which improvessolubility is simultaneously either an electron-donating or -withdrawingsubstituent. One example of such a substituent is a dialkylated aminewith electron-donating action via the nitrogen atom andsolubility-increasing action through the long-chain alkyl groups.

By means of a modular synthesis strategy in which the individual unitsfor preparation of these ligands are combined with one another in amatrix, the introduction of linear and branched and cyclic alkyl chains,alkoxy chains or perfluoroalkyl chains of different length at differentpositions in the molecules is possible. Preference is given tosubstitutions which are far removed from the coordination site of theligand N*∩E.

Proceeding from a suitable synthesis unit A, in analogous reactions,different reactants B, C and D are joined under analogous reactionconditions to give chemically diverse target molecules AB, AC and AD. Itis thus possible, for example, to attach alkyl chains of differentlength to a suitable pyridine ligand in a modular manner by use ofnucleophilic substitution reactions (examples thereof are the ligands ofcomplexes 8,10, 14, see below, in which a central unit has beensubstituted by different substituents under the same reaction conditionsin each case).

For the production of the abovementioned nanoparticles smaller than 30nm, it is possible to employ several techniques:

Bottom-up processes for synthesis of nanoparticles:

-   -   Rapid injection of the reaction solution into a large excess of        a suitable precipitant (e.g. pentane, diethyl ether)    -   Fine atomization of the reaction solution in a vacuum chamber,        possibly at elevated temperature (spray drying). This vaporizes        the solvent, leaving the complex in finely distributed form.    -   In a freeze-drying process, the droplets of the reaction        solution are dispersed in a coolant (e.g. liquid nitrogen),        which freezes the material. Subsequently, it is dried in the        solid state.    -   Codeposition of the complexes and of the matrix material on the        substrate directly from the reaction solution.    -   Synthesis in an ultrasound bath.

Top-down processes for comminution of the substances:

-   -   Comminution by means of high-energy ball mills.    -   Comminution by means of high-intensity ultrasound.

Isolation of the particle size required can be achieved by filtrationwith suitable filters or by centrifugation.

In order to achieve homogeneous distribution of the nanoparticles in thematrix (for example of the matrix material used in the emitter layer), asuspension is prepared in a solvent in which the matrix materialdissolves. The customary processes (for example spin-coating, inkjetprinting, etc.) can be used to apply the matrix material and thenanoparticles to a substrate with this suspension. In order to avoidaggregation of the nanoparticles, stabilization of the particles bymeans of surface-active substances may be necessary under somecircumstances. However, these should be selected such that the complexesare not dissolved. Homogeneous distribution can also be achieved by theabovementioned codeposition of the complexes together with the matrixmaterial directly from the reaction solution.

Since the substances described possess a high emission quantum yieldeven as solids, they can also be deposited directly on the substrate asa thin layer (100% emitter layer) proceeding from the reaction solution.

EXAMPLES

In the examples disclosed here, the ligand E∩N* of the general formula Ais a ligand P∩N* (wherein E=Ph₂P).

For the preparation of the copper complexes, the bidentate phosphineligands 1-3 were used:

While 2-diphenylphosphinylpyridine is commercially available,2-diphenylphosphinylpyrimidine and 1-diphenylphosphinylisoquinoline wereprepared according to eq. 2.

wherein

Ar=py (2); iqn (3)

X=Cl

The identities of compounds 2 and 3 were shown unambiguously by NMRspectroscopy, mass spectrometry, elemental analyses and crystalstructures (see FIGS. 2 and 3).

Examples of Complexes of the Cu₂X₂(P∩N*)₃ Form

I. P∩N*=Ph₂Ppy, 1: Cu₂X₂(Ph₂Ppy)₃, X=Cl (4a), Br (4b), I (4c)

Compounds 4a-4c are yellow, finely crystalline solids.

Characterization:

-   -   Elemental Analyses

found: C 62.48; H 4.40; N 3.90 4a est.: C 62.01; H 4.29; N 4.25 found: C56.89; H 3.93; N 3.90 4b est.: C 57.04; H 3.92; N 3.78 found: C 52.96; H3.94; N 3.50 4c est.: C 52.32; H 3.62; N 3.59.

-   -   The crystal structures are shown in FIG. 4 (4a) and in FIG. 5        (4c).    -   The emission spectra of 4a-4c are shown in FIG. 6.

Since exclusively an identical bidentate ligand in a ratio ofCu:(N*∩E)=2:3 (E=As, P) is used in compounds 4a to 34, complexes of theformula A with extremely intense luminescence are obtained in highyields in a single step. This reduces the synthesis complexity.

II. P∩N*═Ph₂Ppym, 2: Cu₂X₂(Ph₂Ppym)₃, X═Cl (5a), Br (5b), I (5c)

5a-5c are yellow, finely crystalline solids.

Characterization:

-   -   Elemental analyses

found: C 58.45; H 4.12; N 8.43 5a est.: C 58.19; H 3.97; N 8.48. found:C 53.24; H 3.53; N 7.76 5b est.: C 53.40; H 3.64; N 7.78. found: C47.73; H 3.44; N 6.75 5c est.: C 49.12; H 3.35; N 7.16

-   -   The crystal structure is shown in FIG. 7 (5c).    -   The emission specra of 5a-5c are shown in FIG. 8.        III. P∩N*=Ph₂Piqn, 3: Cu₂X₂(Ph₂Piqn)₃, X═Br (6b), I (6c)

6b and 6c are Red, Finely Crystalline Solids.

Characterization:

-   -   Elemental analyses

found: C 60.29; H 4.08; N 3.23 6b (with one DCM molecule) est.: C 59.14;H 2.95; N 3.23 found: C 53.99; H 3.21; N 2.91 6c (with one DCM molecule)est.: C 55.15; H 2.75; N 3.01

-   -   The crystal structure is reproduced in FIG. 9 (6c).    -   The emission spectrum of 6c is shown in FIG. 10. FIG. 11        reproduces the emission decay behavior.        IV. P∩N*=Ph₂Ppic, 7: Cu₂I₂(Ph₂Ppic)₃, 8

Compound 8 is a yellow, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 53.09; H, 3.95; N, 3.39    -   est.: C, 53.48; H, 3.99; N, 3.46    -   The crystal structure is shown in FIG. 14A (8).    -   The emission spectrum of 8 is shown in FIG. 14B.        V. P∩N*=Ph₂P(iBupy), 9: Cu₂I₂(Ph₂P(iBupy))₃, 10

Compound 10 is a yellow, finely crystalline solid. As a result ofintroduction of the isobutyl unit as a substituent of the E∩N* ligand,the solubility is 20-30 mg of complex per ml of dichlorobenzene, whichis sufficient for OLED component production (barely soluble indichlorobenzene without a substituent).

Characterization:

-   -   Elemental analysis:    -   found: C, 56.72; H, 4.96; N, 3.10    -   est.: C, 56.51; H, 4.97; N, 3.14    -   Emission spectrum: see FIG. 15.        VI. P∩N*=Ph₂P(cyPentMepy), 11: Cu₂I₂(Ph₂P(cyPentMepy))₃, 12

Compound 12 is a yellow, finely crystalline solid. As a result ofintroduction of the cyclopentylmethyl unit as a substituent of the E∩N*ligand, the solubility is 30-40 mg of complex per ml of dichlorobenzene,which is sufficient for OLED component production (barely soluble indichlorobenzene without a substituent).

Characterization:

-   -   Elemental analysis:    -   found: C, 58.05; H, 5.04; N, 2.93    -   est.: C, 58.48; H, 5.12; N, 2.97    -   Emission spectrum: see FIG. 16        VII. P∩N*=Ph₂P(heptpy), 13: Cu₂I₂(Ph₂P(heptpy))₃, 14

Compound 14 is a yellow, finely crystalline solid. As a result ofintroduction of the heptyl unit as a substituent of the E∩N* ligand, thesolubility is 35-45 mg of complex per ml of dichlorobenzene, which issufficient for OLED component production (barely soluble indichlorobenzene without a substituent).

Characterization:

-   -   Elemental analysis:    -   found: C, 58.91; H, 5.64; N, 2.85    -   est.: C, 59.02; H, 5.78; N, 2.87

Emission spectrum: see FIG. 17

VIII. P∩N*=Ph₂P(butynpy), 15: Cu₂I₂(Ph₂P(butynpy))₃, 16

Compound 16 is a yellow, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 55.40; H, 4.05; N, 2.95    -   (with one CH₂C12 molecule)    -   est.: C, 57.02; H, 4.10; N, 3.17

Emission spectrum: see FIG. 18

IX. PM*=Ph₂P(4vinylphenpy), 17: Cu₂I₂(Ph₂P(4vinylphenpy))₃, 18

Compound 18 is a yellow, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 60.24; H, 4.59; N, 2.61    -   (with one CH₂Cl₂ molecule)    -   est.: C, 62.31; H, 4.65; N, 2.69    -   Emission spectrum: see FIG. 19        X. P∩N*=Ph₂P(dmap), 19: Cu₂I₂(Ph₂P(dmap))₃, 20

Compound 20 is a white, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 52.39; H, 4.44; N, 6.38    -   est.: C, 52.67; H, 4.42; N, 6.47    -   Crystal structure: see FIG. 20A    -   Emission spectrum: see FIG. 20B        XI. P∩N*=Ph₂P(6Fpy), 21: Cu₂I₂(Ph₂P(6Fpy))₃, 22

Compound 22 is a yellow, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 50.17; H, 3.29; N, 3.42    -   est.: C, 50.02; H, 3.21; N, 3.43    -   Crystal structure: see FIG. 21A    -   Emission spectrum: see FIG. 21B        XII. P∩N*=Ph2P(pyrazine), 23: Cu₂I₂(Ph₂P(pyrazine))₃, 24

Compound 24 is an intensely yellow-colored, finely crystalline solid.

XIII. P∩N*=Ph₂P(6OMepyridazine), 25: Cu₂I₂(Ph₂P(6OMepyridazine))₃, 26

Compound 26 is a yellow/orange-colored, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 47.61; H, 3.56; N, 6.53    -   est.: C, 48.47; H, 3.59; N, 6.65        XIV. P∩N*=Ph₂P(bnzthia), 27: Cu₂I₂(Ph₂P(bnzthia))₃, 28

Compound 28 is a yellow, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 51.19; H, 3.34; N, 3.05    -   est.: C, 51.13; H, 3.16; N, 3.14    -   Crystal structure: see FIG. 22A    -   Emission spectrum: see FIG. 22B        XV. P∩N*=Ph₂P(5Fpy), 29: Cu₂I₂(Ph₂P(5Fpy))₃, 30

Compound 30 is a yellow, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 49.37; H, 3.18; N, 1.76    -   est.: C, 50.02; H, 3.21; N, 3.43    -   Emission spectrum: see FIG. 23        XVI. P∩N*=Ph₂P(Me₂qn), 31: Cu₂I₂(Ph₂P(Me₂qn))₃, 32

Compound 32 is an ochre-colored, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 59.52; H, 4.78; N, 2.73    -   est.: C, 58.98; H, 4.30; N, 2.99    -   Emission spectrum: see FIG. 24        XVII. P∩N*=Ph₂P(quinox), 33: Cu₂I₂(Ph₂P(quinox))₃, 34

Compound 34 is an orange-colored, finely crystalline solid.

Characterization:

-   -   Elemental analysis:    -   found: C, 51.78; H, 3.42; N, 5.84    -   (with one dichloromethane molecule)    -   est.: C, 54.43; H 3.43; N 6.35    -   Emission spectrum: see FIG. 25        Quantum-mechanical Calculations

Proceeding from the crystal structure of 4c, density functional theory(DFT) calculations were conducted at the B3LYP/6-31G(d,p) level.Analogously to the situation in the case of [Cu₂X₂(PPh₃)₂nap], in theground state, the occupied orbitals in the region of the HOMO consistprincipally of Cu and Br orbitals, while the unoccupied orbitals are tobe found in the π-system, in particular of the bridging ligand (FIG.12). On the basis of these results, the origin of the emission istherefore assumed to be a {Cu₂X₂}→π*(ligand) charge transfer state.

FIG. 13 shows an example of an OLED device for the inventive emitterlayer, which comprises an inventive copper(I) complex. For example, in atypical OLED layer structure consisting of an ITO anode, a holeconductor composed of PEDOT/PSS, the inventive emitter layer, optionallya hole-blocking layer, an electron conductor layer, a thin LiF or CsFintermediate layer to improve electron injection and a metal electrode(cathode), good power efficiencies can be achieved. These differentlayers with a total thickness of a few hundred nm can be applied, forexample, to a glass substrate or another carrier material. The layersdisclosed are explained briefly hereinafter:

-   -   1. The carrier material used may be glass or any other suitable        solid or flexible transparent material.    -   2. ITO=indium tin oxide    -   3. PEDOT/PSS (=polyethylenedioxythiophene/polystyrenesulfonic        acid): This is a water-soluble hole conductor material (HTL=hole        transport layer).    -   4. Emitter Layer, frequently abbreviated to EML, comprising        inventive emitter substance. The matrix material of the emitter        layer consists of standard and known materials suitable for this        purpose, for example PVK (polyvinylcarbazole) or CBP        (4,4′-bis(9-carbazolyl)biphenyl). The emitter substance is        applied as a suspension with small particle size (less than 20        to 30 nm), for example by spin-coating.    -   5. ETL=electron transport material (ETL=electron transport        layer). For example, the vapor-depositable Alga can be used.        Thickness, for example, 40 nm.    -   6. The very thin intermediate layer of, for example, CsF or LiF        reduces the electron injection barrier and protects the ETL        layer. This layer is generally applied by vapor deposition. For        a further-simplified OLED structure, the ETL and CsF layers may        optionally be dispensed with.    -   7. The conductive cathode layer is applied by vapor deposition.        A1 represents one example. It is also possible to use Mg:Ag        (10:1) or other metals.    -   The voltage across the OLED device is, for example, 3 to 15 V.

Although illustrative embodiments of the present invention have beendescribed herein with reference to the accompanying drawings, it is tobe understood that the invention is not limited to those preciseembodiments, and that various other changes and modifications may bemade by one skilled in the art without departing from the scope orspirit of the invention.

REFERENCE

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What is claimed is:
 1. An optoelectronic component comprising acopper(I) complex of formula A:

wherein: X=independently selected from Cl, Br and I; N*∩E or E∩N*=abidentate ligand connected to a first Cu atom via an N atom andconnected to a second Cu atom via an E group, or a monodentate ligandconnected to a Cu atom via an E group wherein: E=R₂As or R₂P, wherein Ris selected from the group consisting of alkyl, aryl, alkoxy, andphenoxy; N*=part of an aromatic group comprising an imine functionalgroup, wherein the aromatic group is selected from pyridyl, pyrimidyl,pyridazinyl, triazinyl, oxazolyl, thiazolyl, imidazolyl, and fusedN-heteroaromatics, and wherein the imine functional group comprises theN atom double bonded to a carbon atom of the aromatic group; and ∩=acarbon atom, which is likewise part of the aromatic group, connected tothe N atom of said aromatic group and also connected to the E group viathe As or P atom of the E group.
 2. The optoelectronic component ofclaim 1, wherein the ligands N*∩E and E∩N* of the copper(I) complex areselected from the group consisting of

wherein Y=O, S or NR5 E*=As or P R1-R5 are each independently selectedfrom hydrogen, halogen, substituents bonded via oxygen or nitrogen,alkyl, aryl, heteroaryl, alkenyl, alkynyl, trialkylsilyl, triarylsilyl,alkyl groups substituted by halogens or lower alkyl groups including atleast one of methyl, butyl or propyl groups, aryl groups substituted byhalogens or lower alkyl groups including at least one of methyl, butylor propyl groups, heteroaryl groups substituted by halogens or loweralkyl groups including at least one of methyl, butyl or propyl groups,and alkenyl groups substituted by halogens or lower alkyl groupsincluding at least one of methyl, butyl or propyl groups.
 3. Theoptoelectronic component of claim 2, wherein one or more R group of theligands N*∩E and E∩N* is at least one substituent selected from thegroup consisting of: branched or unbranched or cyclic alkyl chains oflength C1 to C30, branched or unbranched or cyclic alkoxy chains oflength C1 to C30, branched or unbranched or cyclic perfluoroalkyl chainsof length C1 to C30, and short-chain polyethers with a chain length of3-50 repeat units.
 4. The optoelectronic component of claim 1, whereinthe optoelectronic component is in the form of a component selected fromthe group consisting of an organic light-emitting component, an organicdiode, an organic solar cell, an organic transistor, an organiclight-emitting diode (OLED), an OLED sensor, a light-emittingelectrochemical cell, an organic field-effect transistor an organiclaser and a down-conversion element.
 5. The optoelectronic component ofclaim 1, wherein the copper(I) complex is one of an emitter and anabsorber in the optoelectronic component.
 6. The optoelectroniccomponent of claim 5, wherein the proportion of the copper(I) complex inthe emitter or absorber is 100%.
 7. The optoelectronic component ofclaim 5, wherein the proportion of the copper(I) complex in the emitteror absorber is in the range of 1% to 99%.
 8. The optoelectroniccomponent of claim 5, wherein the concentration of the copper(I) complexas an emitter in an optical light-emitting component is between 1% and10%.
 9. The optoelectronic component of claim 1, wherein the copper(I)complex is introduced into a matrix material for conduction of electronsor holes in the optoelectronic component.
 10. The optoelectroniccomponent of claim 9, where the copper(I) complex alters at least one ofan emission property and an absorption property of the optoelectroniccomponent.